Identification of candidate genes of intellectual disability by single-gene deletions/amplifications mapping using chromosomal microarray analysis

INTRODUCTION: Disease-causing deletions/amplifications may include a single gene, several exons or single/part of exon, contributing to detection of novel pathogenic genes. The localization of single-gene deletion/amplification within the gene can affect its clinical manifestation. OBJECTIVES: Impro...

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Detalles Bibliográficos
Autores principales: Kashevarova, A., Lopatkina, M., Belyaeva, E., Fedotov, D., Drozdov, G., Nazarenko, L., Lebedev, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567297/
http://dx.doi.org/10.1192/j.eurpsy.2022.969

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567297/
http://dx.doi.org/10.1192/j.eurpsy.2022.969

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